3‐Methylglutaconic aciduria with persistent metabolic acidosis and ‘uncoupling episodes’
- 1 March 1990
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 13 (2) , 235-236
- https://doi.org/10.1007/bf01799695
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- 3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normalEuropean Journal of Pediatrics, 1988
- A CASE OF SEVERE HYPERMETABOLISM OF NONTHYROID ORIGIN WITH A DEFECT IN THE MAINTENANCE OF MITOCHONDRIAL RESPIRATORY CONTROL: A CORRELATED CLINICAL, BIOCHEMICAL, AND MORPHOLOGICAL STUDYJournal of Clinical Investigation, 1962